| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:136752316-136752716 | Common:1; Rare:128 | ||||
| chr3:136862027-136862298 | Common:1; Rare:82 | ||||
| chr3:138187209-138187560 | Rare:102 | ||||
| chr3:138594191-138594435 | Rare:69 | ||||
| chr3:138834838-138835031 | Rare:68 | ||||
| chr3:139389562-139389876 | Common:2; Rare:102 | ||||
| chr3:139539512-139539751 | Common:3; Rare:86 | ||||
| chr3:140941655-140941911 | Common:2; Rare:98 | ||||
| chr3:141231663-141231899 | Common:2; Rare:82 | ||||
| chr3:141368260-141368556 | Rare:65 | ||||
| chr3:141402262-141402415 | Common:2; Rare:45 | ||||
| chr3:141738096-141738353 | Common:2; Rare:110 | ||||
| chr3:141876049-141876246 | Rare:55 | ||||
| chr3:142447968-142448130 | Common:1; Rare:57 | ||||
| chr3:142578700-142578959 | Rare:97; Clinvar:1; Clinvar (benign):1 |